JPS6045676A - Oil composition for polyamide fiber - Google Patents

Oil composition for polyamide fiber

Info

Publication number
JPS6045676A
JPS6045676A JP15057883A JP15057883A JPS6045676A JP S6045676 A JPS6045676 A JP S6045676A JP 15057883 A JP15057883 A JP 15057883A JP 15057883 A JP15057883 A JP 15057883A JP S6045676 A JPS6045676 A JP S6045676A
Authority
JP
Japan
Prior art keywords
dyeing
oil
agent
oil composition
dye
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP15057883A
Other languages
Japanese (ja)
Other versions
JPS6317149B2 (en
Inventor
清一 越智
福岡 重紀
一郎 吉田
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Toyobo Co Ltd
Original Assignee
Toyobo Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Toyobo Co Ltd filed Critical Toyobo Co Ltd
Priority to JP15057883A priority Critical patent/JPS6045676A/en
Publication of JPS6045676A publication Critical patent/JPS6045676A/en
Publication of JPS6317149B2 publication Critical patent/JPS6317149B2/ja
Granted legal-status Critical Current

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Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 本発明はポリアミド系繊維用油剤組成物に関するもので
あり、更に詳しくけ均染性、再汚染防止性等にすぐt′
したポリアミド繊維を94することを目的とした油剤組
成物に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an oil composition for polyamide fibers.
The present invention relates to an oil composition intended to coat polyamide fibers.

従来、ポリアミド繊維はすぐれた力学的特性、常圧可染
性の長所を有し、一般衣料品以外にインテリア製品、自
動車内装品等の広範囲の分野で1史用されている。一般
にポリアミド繊維は特殊用途のドープ染色(原着)を除
外すれば、酸性染料。
Conventionally, polyamide fibers have the advantages of excellent mechanical properties and dyeability under normal pressure, and have been used in a wide range of fields such as interior products and automobile interior products in addition to general clothing. In general, polyamide fibers are made with acid dyes, except for dope dyeing (dope dyeing) for special purposes.

含金染料VC代表されるアニオン性染料で染色されるの
が通常である。しかしながら、このような染色において
は次の如き欠点があった。すなわち、(1)染着座席量
(ポリアミドのアミド末端基」)の変動および/または
繊維の外観形状特性(捲縮特性、光沢など)差に起因す
ると考えられているたす てすじ(スト%−り)が発生し易いこと、(2)染色物
から脱落したアニオン性染料の白湯(未染色部)への再
汚染の発生により製品の外観品位を著しく低下させるこ
と等である。
It is usually dyed with an anionic dye such as metal-containing dye VC. However, such dyeing has the following drawbacks. In other words, (1) the amount of staining (streak % (2) The anionic dye that has fallen off from the dyed product recontaminates the hot water (undyed area), which significantly deteriorates the appearance quality of the product.

従来、ポリアミド繊維の均染性を得るためにはθ近1を
層別の徹底により染着座席量の変動の小さb1+JC糸
の使用と染色条件のi4足(均染性にすぐれたηυ科の
使用、PHコントロール、均染剤の添加、昇温スピード
のコントロール等)が行われている。
Conventionally, in order to obtain level dyeing properties of polyamide fibers, thorough layering of θ near 1 was used to minimize fluctuations in the dyed seat amount, and the use of b1 + JC yarns and the use of i4 pairs of dyeing conditions (ηυ family with excellent level dyeing properties) use, PH control, addition of leveling agent, temperature increase speed control, etc.).

しかじなが゛ら、層別に長時間を必要とすること、均染
性のすぐ7′した染料は染色堅牢度が劣ること、P T
iコントロール、昇温スピードコントロールおよび均染
剤を添加する方法はある程度の均染効果は4UらI]る
が高ずのコントロール技術が要求され7Lす、染色時間
に長時間を必要としたり、再現性に乏1−いなどの欠点
を有し、工業的な有用性は小さい。−また、再汚染防止
性のためには湿潤堅牢度のすぐi’した染料を使用−す
る方法、充分なソーピング後フィックス処理する方法か
あるが、使用染料のjlill約が大六いこと、ソーピ
ング番で時間がかかる等の欠点を有し実用性に欠ける。
However, the disadvantages are that it takes a long time to separate the layers, that dyes with a quick level dyeing property have poor color fastness, and that P.T.
Methods such as i control, temperature increase speed control, and adding a leveling agent can achieve a certain degree of leveling effect from 4U to 7L, but they require a high level of control technology, require a long dyeing time, and are difficult to reproduce. It has drawbacks such as poor properties and is of little industrial utility. -Also, in order to prevent re-staining, there is a method of using a dye with a high wet fastness, and a method of fixing after thorough soaping, but it is important to note that the dye used is approximately It has drawbacks such as time-consuming process and lacks practicality.

本発明者等は上記欠点のない均染化および再汚染防止法
につき鋭意研究の結果、油剤中に特定の処理剤を配合し
処理することにより均染性および再汚染防止性が得られ
ることを知見【−1本発明の油剤組成物に到達した。す
なわち、本発明は分子中に少くとも1個のフェノール性
水酸基と少くとも1個のスルホン酸基を有する芳香族ス
ルホン酸縮合物および油剤を含有してなることを特徴と
するポリアミド系繊維用油剤組成物である。
As a result of intensive research into a method for leveling dyeing and preventing re-staining that does not have the above-mentioned drawbacks, the present inventors have discovered that level dyeing and re-staining prevention properties can be obtained by blending a specific treatment agent into the oil agent. Findings [-1] The oil composition of the present invention was achieved. That is, the present invention provides an oil agent for polyamide fibers characterized by containing an aromatic sulfonic acid condensate having at least one phenolic hydroxyl group and at least one sulfonic acid group in the molecule and an oil agent. It is a composition.

本発明において用いられる分子中に少くとも1個のフェ
ノール性水酸基と少くとも1個のスルホン酸基を有する
芳香族スルホン酸縮合物としては、シンタン類が挙げら
れる。具体的にはフェノールスルホン酸のホルムアルデ
ヒド縮金物、ノボラック型樹脂のメタンスルホン酸、レ
ゾール型樹脂のメタンスルホン酸、フェノール類トナフ
タレンスルホン酸をホルムアルデヒドと共に縮合させて
得られる樹脂等も例示されるが、特に下記一般式(1)
で示される化合物が好ましい。
Examples of the aromatic sulfonic acid condensate having at least one phenolic hydroxyl group and at least one sulfonic acid group in the molecule used in the present invention include syntanes. Specific examples include formaldehyde condensates of phenolsulfonic acid, methanesulfonic acid as novolac type resins, methanesulfonic acid as resol type resins, and resins obtained by condensing phenols tonaphthalenesulfonic acid with formaldehyde. In particular, the following general formula (1)
Compounds represented by are preferred.

X:ベンゼン環、ナフタレン環 Y・−so、−、−5o−、−5−1炭素数6以下のア
ルキレン基、アルキリデン基または2個のXが直接結合
し2ていてもよい。
X: benzene ring, naphthalene ring Y.-so, -, -5o-, -5-1 alkylene group having 6 or less carbon atoms, alkylidene group, or two Xs may be directly bonded to each other.

Z : −CF(tsOsM、 −808M、 −OH
,−CH,OH才たは炭巣赦1〜18のアルキル基であ
り、少くとも1個ki CH25,OsM、505Mで
ある。
Z: -CF(tsOsM, -808M, -OH
, -CH,OH or an alkyl group of 1 to 18, and at least one ki CH25, OsM, 505M.

o+ : ]〜4の整数 n:l〜9の整数 )71=アルカリ金絹 し4v(具体例としてに1下記の化合物が例示される。o+: ]~4 integer n: integer from 1 to 9 )71=alkali gold silk 4v (Specific examples include the following compounds.

しかしながら、無色でポリアミド’fj(kJeのカチ
オン染料座席(アミノ基)とイオン結合できる酸性染料
又はg今染料Vζ対l−でL!::染効果を有する水溶
性丑たけ水分散性化合物であれば特にら1j限されるも
のではない0.芳香族スルホン[没化合物の分子廿Vi
酸性染料、k全染料のj采効果またtよ再汚染防止効果
に大きく影響する因子の一つであり、均染性改善用と1
−ではポリアミド繊維に対する使用染料の親和力よりや
\小’J ’−’1化合物が、また丹汚染防止用として
は使用染料の親オΩ力より大きい化合物が好ましい。該
化合物rt2釉以上の併用であってもtい。
However, acidic dyes that are colorless and capable of ionically bonding with the cationic dye sites (amino groups) of polyamide 'fj (kJe) or g-now dyes Vζ vs. In particular, but not limited to, 0. aromatic sulfone [molecules of the compound
It is one of the factors that greatly affects the re-staining prevention effect of acid dyes and total dyes.
- For polyamide fibers, it is preferable to use a compound whose affinity is smaller than that of the dye used, and for prevention of red staining, it is preferable to use a compound whose affinity is larger than that of the dye used. The compound may be used in combination with two or more glazes.

芳香族スルホンに化合物と所望によυ配3−さtLる膨
潤剤としては、ブチルアルコール、エチレングリコール
のような一価アルコール走た(、i多1111Iアルコ
ール類およびそれらの変性吻、フェニルフェノール、安
息香酸メチル、サリチル酸メチル、7タル岐ジエチル、
フェノールスルホン酸、ベンジルアルコールのような芳
香族化合物類などが挙げられるが、アルコール傾が好−
ましく、就中ベンジルアルコールが特に好′まし、い。
Swelling agents optionally combined with aromatic sulfone compounds include monohydric alcohols such as butyl alcohol, ethylene glycol, polyalcohols and their modified forms, phenylphenol, Methyl benzoate, methyl salicylate, 7-tal diethyl,
Examples include aromatic compounds such as phenolsulfonic acid and benzyl alcohol, but alcohol-based compounds are preferred.
Of these, benzyl alcohol is particularly preferred.

エステル系平滑剤全部用しないときは膨潤剤を配合する
のが好ましい。
When the ester leveling agent is not used at all, it is preferable to add a swelling agent.

“また配合される油剤としては、たとえば紡糸、延伸、
lj74%加工およびその他後工程の生産性、性能を維
持するため、潤滑性、制電性、集束性およびヒーター上
での熱分解に耐える耐熱性等の要求!特性を満足【7な
け几ばならない。このような要求特性を値足するものと
しては、−塩基酸エステル+11、二地基酸エステル類
、多塩基酸エステル類、タリコールエステルI’b(、
多価アルコールエステルノメシなどのエステル系平滑剤
が挙げられるが、脂肪i+にm=塩基酸のジアルキルエ
ステル類力;好ましく、14体的にはジプロピルセバケ
ート、ジラウリルセバケート、ジラウリルアジペートな
どが例示される。エステル系平滑剤はポリアミドの膨潤
剤としての作用も有する。また、油剤として鉱1勿油、
シリコーン油などの液状油剤も用いることができ、これ
らの中では高粘度鉱物油が好゛ましい。上記エステル系
嘔滑剤と液状油剤とを併用−「るのが特に好捷しい。捷
た、油剤は所望により非イオン系の乳化剤や制′屯剤た
とえば高級アルコールや高級脂肪峻、高級脂肪酸アミド
などのアルギレンオギシド付加体プルロニック型活性剤
などをυト用l−で用いら名、る。
“Furthermore, the oil agents that can be blended include, for example, spinning, stretching,
In order to maintain the productivity and performance of lj74% processing and other post-processes, requirements include lubricity, antistatic properties, focusing properties, and heat resistance to withstand thermal decomposition on the heater! Satisfy the characteristics [Must be 7. Examples of substances that meet these required properties include -basic acid esters +11, dibasic acid esters, polybasic acid esters, and tallicol esters I'b (,
Examples include ester smoothing agents such as polyhydric alcohol esters, but fatty acids (i+) and (m) = dialkyl ester of basic acid; preferred examples include dipropyl sebacate, dilauryl sebacate, and dilauryl adipate. Examples include. The ester leveling agent also functions as a swelling agent for polyamide. Also, as an oil agent, mineral oil,
Liquid oils such as silicone oil can also be used, and among these, high viscosity mineral oil is preferred. It is particularly preferable to use the above ester-based lubricant in combination with a liquid oil agent. Argylene oxide adducts, pluronic type activators, and the like are used in the l- for use.

本発明における油剤組成物は有効成分と1−7て芳香族
スルホン酸縮合物3〜60重量%、11.脣潤剤0〜1
5重吋係好オしくu5〜15重All値、油剤10〜4
0重j−,%、残部が非イオン系乳化剤からなり、該油
剤を適宜稀釈し通常3〜50−Bi7 :f%、史には
5〜20゛は骨チとして用いるのが好−il、い。
The oil composition of the present invention contains 1-7 active ingredients, 3-60% by weight of an aromatic sulfonic acid condensate, 11. Moisturizer 0-1
5 weight ratio, u5~15 weight All value, oil agent 10~4
0 weight j-,%, the balance consists of a nonionic emulsifier, the oil agent is diluted appropriately and usually 3 to 50-Bi7: f%, in history 5 to 20゛ is preferably used as a bone filtrate, stomach.

なお、油剤成分におけるエステル系平滑剤と液状油剤と
の割合は15〜80:85〜20 M 、’lit比が
好まl−’y’h 。
In addition, the ratio of the ester smoothing agent and the liquid oil agent in the oil agent component is preferably 15-80:85-20 M, and the 'lit ratio is l-'y'h.

本発明の油剤組成物はポリアミド系の)板維、または糸
、ことに未延伸繊維に公知の方法、たとえげローラ伶布
、浸漬、撒布等の手段により付与し、〈・賦沖する紡糸
油剤として用いるのが好適である。
The oil composition of the present invention is applied to polyamide-based fibers or threads, especially undrawn fibers, by known methods such as rolling, dipping, and spraying. It is suitable to use it as

刀、a用されるポリアミド繊維としては、羊毛、絹、P
の天然ポリアミド繊維も挙げられるが、特にす・(rJ
ン6、ナイロン616、ナイロン11、ナイロン12、
芳香族ナイロンのような合成ポリアミド繊維、蛋白・ア
クリロニトリル共重合体繊維等に適用して好結果を得る
ことができる。
Polyamide fibers used for swords and a include wool, silk, and P.
Natural polyamide fibers such as
N6, Nylon 616, Nylon 11, Nylon 12,
Good results can be obtained when applied to synthetic polyamide fibers such as aromatic nylon, protein/acrylonitrile copolymer fibers, and the like.

本発明における芳香族スルホン酸縮合物は均染性、再汚
染防止性を改良するが、エステル系平滑j+lI ’ま
fcは/および膨潤剤の併用によって芳香族スルホン藏
縮8−物の繊維内部への浸透が助長され、すぐれた均染
効果を与えることができる。膨潤剤1(i±だ油剤の内
部浸透を助長することもできる。
The aromatic sulfonic acid condensate in the present invention improves the level dyeing property and re-staining prevention property, but the ester-based smooth j+lI' mafc can be applied in combination with the aromatic sulfonic acid condensate to the inside of the fiber. This facilitates the penetration of the dye, giving an excellent level dyeing effect. Swelling agent 1 (i±) can also promote internal penetration of the oil agent.

?tll 剤1115分の中ニスデル系平滑剤はまた糸
状の集束性、紡糸延伸性、後工程通過性、耐摩耗性を改
良するのVC有効でちり、液状油剤は紡糸、延伸、捲4
:+7 fiどの諸工程における平滑性改良に有効であ
る。
? Tll agent 1115 minutes Nisder type smoothing agent is also VC effective for improving filament cohesiveness, spinning drawability, post-process passability, abrasion resistance, and liquid oil agent is used for spinning, drawing, winding 4.
:+7 Effective for improving smoothness in various processes.

【、たがって、本発明の油剤組成物によって処理さJ′
L7cポリアミド繊維は紡糸延伸性、後工程通過性が改
善され、良好な耐・摩耗性とすぐれた均染性、耐汚染防
止性を有しており、精疎等の前処理を励すことなく、そ
のままかつ短時間染色でさえすぐれた均染性が得られる
こと、捺染後のソーピング時に白湯への汚染が防1Fさ
れること、染色糸と未染色糸の交編織布帛の洗瘤および
着用時にブリードアウトした染料による未染色糸の汚染
がないこと、芳香族スルホン酸縮合物無添加油剤による
処理繊維との混用により単−染料使いでd淡効呆が得ら
れることなど多くの特長を有している。
[, Therefore, J′ treated with the oil composition of the present invention
L7c polyamide fiber has improved spinning drawability and post-process passability, good abrasion resistance, excellent level dyeing properties, and stain resistance, and can be processed without requiring pretreatment such as fine graining. , excellent level dyeing properties can be obtained even when dyed as is and for a short period of time, contamination of hot water during soaping after printing is prevented, 1F is effective when washing and wearing mixed knitted fabrics of dyed and undyed yarns. It has many features such as no contamination of undyed yarn by dye that bleeds out, and the ability to obtain a d-light effect even when using a single dye by mixing it with fibers treated with aromatic sulfonic acid condensate additive-free oil agents. ing.

本発明の油剤組成物によりすぐれた均染性および再汚染
防止性が得られる理由については不明確であるが、原糸
製造段階でυ染効果を有する特定のアニオン性化合物を
エステル系平滑?IJ 公よび/またけ膨潤剤と共に使
用することにより、アニオン性化合物が繊維衣面層内部
νこ、しかも1哉J、I:1本1本に均一に付2u1〜
でいること、およびアニオン性化合物と使用染料(アニ
オン性染料)のは維pc対する親和力の大小により均染
幼果−、+ ′fLけ再汚染防止効果が得られるためと
考えられろ。
Although it is unclear why the oil composition of the present invention provides excellent level dyeing properties and redeposition prevention properties, it is unclear why the oil composition of the present invention provides excellent level dyeing properties and re-staining prevention properties. By using IJ with a swelling agent, an anionic compound can be applied evenly to the inside of the fiber coating layer, and evenly applied to each fiber.
This is thought to be due to the fact that the anionic compound and the dye used (anionic dye) have an effect of preventing recontamination of evenly dyed young fruits depending on the affinity for fiber PC.

本発明の油剤組成物にjri、更に所望により螢光染料
、ン味付染料、防黴剤、紫外線吸収剤等−を配合゛i−
ることもでさる。
The oil composition of the present invention may further contain fluorescent dyes, flavoring dyes, fungicides, ultraviolet absorbers, etc., if desired.
It's also possible.

なお、ポリアミド用均染剤としては、染料に親ill 
(′i−(、−有するカチオン性化合物の使用も考えら
れるが、紡糸油剤ご二の相溶性、染色時における染料と
のコンプレックス形成および変色の問題等を有す、・5
ことから不〕i当である。
In addition, as a leveling agent for polyamide, it is suitable for dyes.
('i-(, -) Although it is possible to use a cationic compound having -, it has problems such as compatibility with the spinning oil, complex formation with the dye during dyeing, and discoloration.
Therefore, it is inappropriate.

以下、実施例Vこより本発明を説明する。なお、実施例
中の部は重1檜部を意味する。
The present invention will be explained below with reference to Example V. In addition, the part in an Example means a 1-hinoki cypress part.

尖ノj、)1例1 アミノ末婦基°トドの¥4なる3種のナイロン6樹脂4
−夫々[天川し、常法によV浴融紡糸して得られる:う
撞の未延伸繊kin vc第1表に示した紡糸油剤を各
機AIL糸条(濃染タイプ:■、普通タイプ:■、淡染
タイプ、O)に対し、4重量%付与し延伸、捲[,11
力■工1.てナイロンBCF (800d/64f )
を得た。
3 types of nylon 6 resin 4 consisting of ¥4 of amino terminal group° sea lion
- Each machine AIL yarn (dark dyed type: ■, normal type) using the spinning oil shown in Table 1. :■, Light dyed type, O), 4% by weight was added and stretched and rolled [,11
Power ■Work 1. Nylon BCF (800d/64f)
I got it.

イ(Jらハ、た糸をタフトマシーンを使用して■、■、
Oが夫々隣り合わせとなるように基布にタフティングし
、ループパイルカーペア)を得た。次いで酸性染料また
は合金染料によりウィンス染色後、常法によりバッキン
グ剤を裏打ち[また。得られたループパイルカーペット
の均染性を標価し、結果を第1表に示した。
I (Jraha, use the tufting machine to make the yarn ■, ■,
The base fabric was tufted so that the O's were adjacent to each other to obtain a loop pile carpet. Then, after wince dyeing with an acid dye or an alloy dye, a backing agent is applied by a conventional method. The level dyeing properties of the obtained loop pile carpets were evaluated and the results are shown in Table 1.

笛1表 3) g)V性染料染色処方と条件 C,1,アシッドエロー 380゜5φowfC,1,
アシッドレッド145 0.1%IC,1,アシッドブ
ルー40 0.05%I酢iz2 (9(1% ) 0
−5ceAh消・12ソーダ 2 y/1 染色沃■(均染剤なし) 染色法■ (均染剤あり) b)含金染料染色処方と電性 Lanyl Yellow G ’ 0 、i%owf
(住人rヒ学社 1:2型含金染相) TJanyI Blue G (1,5%oXvf(住
友什学社1:2型含、獅染料) 酢酸 0゜5C/e 酢θソーダ 2y、’l 均染剤 0.5%owf 染色法の、■および均染剤は 酸性染料の場合と同じ ・なお、染着座席の差違■、@、(On下’MI2処方
の染浴中、浴比1 : iuo、ボイル60分染色り、
、(Blの染着率f標準として■は+1受(淡染)、■
+(1−1%(淡染)異なる。また、均染性像側ばの、
■、Oの架設、ストリークの根囲を目視判定して行った
Flute 1 Table 3) g) V dye staining prescription and conditions C, 1, Acid Yellow 380°5φowfC, 1,
Acid Red 145 0.1% IC, 1, Acid Blue 40 0.05% I Vinegar iz2 (9 (1%) 0
-5ceAh extinguisher/12 soda 2 y/1 Dyeing method■ (without leveling agent) Dyeing method■ (with leveling agent) b) Gold-containing dye dyeing recipe and electrolytic Lanyl Yellow G' 0, i%owf
(Sumitomo Ji Gakusha 1:2 type gold-containing dye phase) TJanyI Blue G (1,5%oXvf (Sumitomo Ji Gakusha 1:2 type, Shi dye) Acetic acid 0゜5C/e Vinegar θ Soda 2y,' l Leveling agent 0.5%owf The dyeing method, ■ and the leveling agent are the same as for acid dyes.The difference in the dyeing seat is ■, @, (On below' in the dye bath of MI2 prescription, the bath ratio 1: iuo, boil 60 minute dyeing,
, (Bl dyeing rate f standard: ■ is +1 (light dyeing), ■
+ (1-1% (light dyeing) difference. Also, the level dyeing image side part,
(2) Erection of O was carried out by visual judgment of the root circumference of the streak.

その結果、比較例は均染性が得られず、均染剤のんジ度
を増加L7ても改善さ力、なかった。一方、本)1.明
による油剤、ことに膨簡剤を併用したものば「ぐれた均
染性を与えた。
As a result, in the comparative example, level dyeing property was not obtained, and even if the leveling agent leveling degree was increased to L7, there was no improvement. On the other hand, books) 1. The use of oil agents by Ming Dynasty, especially those combined with swelling agents, gave ``excellent level dyeing properties.''

実hiIr例2 A b市例1と同様にして、実施例1における油剤rr
a l ’47用イー(A4jらり、 e す4076
 BCF (50d /12f )、λ5、=糸条■と
油剤屋3を用いて得られたナイロン(i BCF (5
(ld/12f)繊IJL糸条■とを白湯形成繊維と1
1.て使用し、油剤A1を使用して得らねたナイロンr
i BCF先染糸を色地形成繊絣として使用して先染ス
トライプ柄の交編jLr、を作bZ後、汗堅牢度(JI
SL −0848A法)およびJISL −0844A
 −2号による洸潤時の染色糸から未染色糸(白湯〕へ
の染料のlす(代1生をm個1した。
Actual hIr Example 2
a l '47 e (A4j rari, e su4076
BCF (50d/12f), λ5, = nylon (i) obtained using yarn
(ld/12f) Fiber IJL yarn ■ and white water forming fiber 1
1. Nylon r obtained using oil agent A1
i Using BCF yarn-dyed yarn as a colored ground-forming fiber kasuri, cross-knit jLr with a yarn-dyed stripe pattern was created. After bZ, sweat fastness (JI
SL-0848A method) and JISL-0844A
-1 dye was added from the dyed yarn to the undyed yarn (white water) during dyeing using No. 2.

その結果、本発明油剤処理繊維への先染糸からの71j
染は見ら゛)′1、ないのに対し、比較例油剤処理繊A
、、への汚染は著しく、本発明の油剤がすぐれた汚q′
−防IEtb来をもつことを示l−だ。
As a result, 71j from the yarn-dyed yarn to the oil-treated fiber of the present invention
No dyeing was observed in Comparative example oil treated fiber A.
, , is significant, and the oil agent of the present invention has excellent stain
- Indicates that it has an anti-IEtb characteristic.

Claims (1)

【特許請求の範囲】 1 分子中に少くとも1個のフェノール性水酸基と少く
とも1個のスルホン酸基を有する芳香族スルホン酸縮合
物および油剤を含有してなることf特徴とするポリアミ
ド系繊維用油剤組成物。 2 芳香族スルホン酸縮合物が一般式(1)で示さrし
る化合物である特許請求の範囲第1項記載のポリアミド
系繊維用油剤組成物。 X、ベンゼン環、ナフタレン環 yニー5O2−1−so−1−s−1炭素数6以下のア
ルキレン基、アルキリデン基、2個のXがi&接結合し
ていてもよい。 Z : −8o、M、 −CH,SO,M、 −0H1
CHtOH−Cめり、少くとも1個は一8O,M、 −
CH,80,Mである。 mal〜4の整数、 nil〜9の整数M:アルンノリ
金属
[Scope of Claims] 1. A polyamide fiber characterized by containing an aromatic sulfonic acid condensate having at least one phenolic hydroxyl group and at least one sulfonic acid group in the molecule and an oil agent. Oil composition for use. 2. The oil composition for polyamide fibers according to claim 1, wherein the aromatic sulfonic acid condensate is a compound represented by general formula (1). X, a benzene ring, a naphthalene ring, an alkylene group having 6 or less carbon atoms, an alkylidene group, and two Xs may be bonded together. Z: -8o, M, -CH,SO,M, -0H1
CHtOH-C, at least one is -8O,M, -
CH, 80, M. Integer from mal to 4, Integer from nil to 9 M: Arun Nori metal
JP15057883A 1983-08-18 1983-08-18 Oil composition for polyamide fiber Granted JPS6045676A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP15057883A JPS6045676A (en) 1983-08-18 1983-08-18 Oil composition for polyamide fiber

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP15057883A JPS6045676A (en) 1983-08-18 1983-08-18 Oil composition for polyamide fiber

Publications (2)

Publication Number Publication Date
JPS6045676A true JPS6045676A (en) 1985-03-12
JPS6317149B2 JPS6317149B2 (en) 1988-04-12

Family

ID=15499940

Family Applications (1)

Application Number Title Priority Date Filing Date
JP15057883A Granted JPS6045676A (en) 1983-08-18 1983-08-18 Oil composition for polyamide fiber

Country Status (1)

Country Link
JP (1) JPS6045676A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1995011331A1 (en) * 1993-10-18 1995-04-27 Interface, Inc. Treatment for imparting stain resistance to polyamide substrates and resulting stain resistant materials

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH03118958U (en) * 1990-03-22 1991-12-09
JPH0572847U (en) * 1992-03-11 1993-10-05 株式会社新興製作所 Conveyance guide mechanism for paper sheets
JPH0743738U (en) * 1994-03-23 1995-09-05 ブラザー工業株式会社 Document reader

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5020100A (en) * 1973-06-29 1975-03-03

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5020100A (en) * 1973-06-29 1975-03-03

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1995011331A1 (en) * 1993-10-18 1995-04-27 Interface, Inc. Treatment for imparting stain resistance to polyamide substrates and resulting stain resistant materials

Also Published As

Publication number Publication date
JPS6317149B2 (en) 1988-04-12

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